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Clinical trial of efficacy and safety of sekukizumab in the treatment of HIV-infected patients with psoriasis

Clinical trial of efficacy and safety of sekukizumab in the treatment of HIV-infected patients with psoriasis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300074833
Enrollment
Unknown
Registered
2023-08-17
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

psoriasis

Interventions

Sekukuniumab treatment group:NA
Routine treatment group for psoriasis (topical medication+acitretin):NA

Sponsors

First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-70 years old, male or female. (2) Diagnosed with HIV infection combined with psoriasis (moderate to severe plaque psoriasis, pustular psoriasis, erythrodermic psoriasis, articular psoriasis), diagnosed by at least 2 deputy chief physicians, according to the "Chinese Psoriasis Diagnosis and Treatment Guidelines (2018 Edition)" and "China AIDS Diagnosis and Treatment Guidelines (2021 Edition)". (3) Those who receive and can adhere to antiviral therapy (ART). (4) HIV viral load was lower than the lower limit of detection (50 copies/ml), CD4+ T cell count > 200 cells/µl. (5) Be able to understand and voluntarily sign written informed consent. Be able to complete treatment and follow-up as required.

Exclusion criteria

Exclusion criteria: (1) Those who have used glucocorticoids or immunosuppressants in the past 4 weeks. (2) Those with other infectious diseases, such as active hepatitis, tuberculosis, etc. (3) Combined with other skin diseases, such as systemic lupus erythematosus, dermatomyositis, pemphigus, pemphigoid, etc. (4) Patients with tumors. (5) Psychiatric illness or disease of the nervous system (cognitive impairment) that affects the assessment. (6) Pregnant women or breastfeeding women.

Design outcomes

Primary

MeasureTime frame
PASI score;BSA score;DLQI score;

Countries

China

Contacts

Public ContactLi yuye

First Affiliated Hospital of Kunming Medical University

yyeli2000@126.com+86 139 8716 5540

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026